NZ561399A

NZ561399A - Method for preparation of optionally 2-substituted 1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acids

Info

Publication number: NZ561399A
Application number: NZ561399A
Authority: NZ
Inventors: Rafael Shapiro
Original assignee: Du Pont
Priority date: 2005-05-06
Filing date: 2006-04-28
Publication date: 2009-11-27
Also published as: DK1877384T3; CN101171237B; DE602006021411D1; WO2006121648A2; GEP20105099B; US20120232271A1; MX2007013424A; EP1877384A2; CN102153516A; US8198442B2; ATE506352T1; UA92171C2; KR101379967B1; ES2362005T3; EG25480A; ME00498B; CN102153516B; BRPI0612475B8; CN101171237A; IL185885A

Abstract

Disclosed is a method of preparing a compound of formula (I). Also disclosed are methods comprising additional steps to prepare optionally substituted 4 pyrimidine-carboxylic acids and esters using the compound of formula (I) as an intermediate.

Description

<div class="application article clearfix" id="description"> New Zealand Paient Spedficaiion for Paient Number 561 399 WO 2006/121648 561399 PCT/US2006/016340 1 TITLE METHOD FOR PREPARATION OF OPTIONALLY 2-SUBSTITUTED 1,6-DIHYDRO-6-OXO-4-PYRIMIDINECARBOXYLIC ACIDS FIELD OF THE INVENTION 5 A new method for the preparation of optionally 2-substituted l,6-dihydro-6-oxo- 4-pyrimidinecarboxylic acids is disclosed. BACKGROUND OF THE INVENTION G. D. Daves, Jr. et al. (J. Org. Chem., 1961, 26, 2755) disclose a preparation of l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid by cyclocondensation of diethyl oxalacetate 10 with formamidine in aqueous NaOH. In their procedure, the components were combined all at once without particular control of pH to provide a yield of 63 %. Other reports on similar condensations using oxalacetate diesters disclose even lower yields. Therefore new methods are needed to provide higher yields as well as affording low cost, high efficiency, and reliability. 15 SUMMARY OF THE INVENTION This invention provides a method for preparing a l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid compound of Formula 1 20 wherein R1 is H or an optionally substituted carbon moiety; comprising the steps of: (1) contacting a mixture comprising (a) a compound of Formula 2a R2o2c. _ , CO,R3 OM 2a 25 wherein M is alkali metal and R2 and R3 are independently Cj-C4 alkyl, (b) a C1-C4 alkanol, and (c) a first portion of water, with a solution comprising a first base and a second portion of water, said base being in an amount sufficient to create a first resultant solution having a pH ranging from about 10 to about 14, said first resultant solution comprising a compound of Formula 2b, WO 2006/121648 561399 PCT/US2006/016340 M02C>. , XO2R3 OM 2b wherein M and R3 are defined as above for Formula 2a; (2) contacting the first resultant solution comprising the compound of Formula 2b with 5 a compound of Formula 3 or an acid salt thereof or with a solution comprising a compound of Formula 3 or an acid salt thereof, NH X R1 NH2 3 wherein R1 is defined as above for Formula 1, and a second base in an amount sufficient to 10 create a second resultant solution having a pH ranging from about 9 to about 12, said second resultant solution comprising a salt of the compound of Formula 1; and (3) adding an acid to the second resultant solution comprising the salt of the compound of Formula 1 to form the compound of Formula 1. The invention also provides a method for preparing the compound of Formula 4 O J^^ci HN 15 R1 N C02H 4 wherein R1 is H or an optionally substituted carbon moiety, comprising the aforedescribed method and an additional step of contacting the compound of Formula 1 with a chlorinating agent. The invention also provides a method for preparing the compound of Formula 6 CI IT R1 N>^C02H 20 6 wherein R1 is H or an optionally substituted carbon moiety, WO 2006/121648 561399 PCT/US2006/016340 3 comprising the aforedescribed method and an additional step of contacting the compound of Formula 4 with a chloride displacement agent. The invention also provides a method for preparing the compound of Formula 7 5 wherein R* is H or an optionally substituted carbon moiety, comprising the aforedescribed method and an additional step of contacting the compound of Formula 6 with ammonia. The invention also provides a method for preparing the compound of Formula 8 8 10 wherein R1 is H or an optionally substituted carbon moiety; and R4 is an optionally substituted carbon moiety; comprising the aforedescribed method and an additional step of contacting the compound of Formula 7 with an R4 transfer agent. Accordingly, the invention also provides a method for preparing a compound of 15 Formula 4 using a compound of Formula 1, characterized by preparing the compound of Formula 1 from the compounds of Formulae 2a and 3 by the 'aforedescribed method. The invention also provides a method for preparing a compound of Formula 6 using a compound of Formula 1, characterized by preparing the compound of Formula 1 from the compounds of Formulae 2a and 3 by the aforedescribed method. The invention also provides a method 20 for preparing a compound of Formula 7 using a compound of Formula 1, characterized by preparing the compound of Formula 1 from the compounds of Formulae 2a and 3 by the aforedescribed method. The invention also provides a method for preparing a compound of Formula 8 using a compound of Formula 1, characterized by preparing the compound of Formula 1 from the compounds of Formulae 2a and 3 by the aforedescribed method. 25 DETAILED DESCRIPTION OF THE INVENTION In the recitations herein, the term "carbon moiety" refers to a radical comprising a carbon atom linking the radical to the remainder of the molecule. As the substituent R1 is WO 2006/121648 561399 PCT/US2006/016340 separated from the reaction center and R4 is added at the end of the disclosed sequence of steps, R1 and R4 can encompass a great variety of carbon-based groups preparable by modern methods of synthetic organic chemistry. "Carbon moiety" thus includes alkyl5 alkenyl and alkynyl, which can be straight-chain or branched. "Carbon moiety" also 5 includes carbocyclic and heterocyclic rings, which can be saturated, partially saturated, or completely unsaturated. Furthermore, unsaturated rings can be aromatic if Huckel's rule is satisfied. The carbocyclic and heterocyclic rings of a carbon moiety can form polycyclic ring systems comprising multiple rings connected together. The term "carbocyclic ring" denotes a ring wherein the atoms forming the ring backbone are selected only from carbon. 10 The term "heterocyclic ring" denotes a ring wherein at least one of the ring backbone atoms is other than carbon. "Saturated carbocyclic" refers to a ring having a backbone consisting of carbon atoms linked to one another by single bonds; unless otherwise specified, the remaining carbon valences are occupied by hydrogen atoms. The term "aromatic ring system" denotes fully unsaturated carbocycles and heterocycles in which at least one ring in 15 a polycyclic ring system is aromatic. Aromatic indicates that each of ring atoms is essentially in the same plane and has a j>-orbital perpendicular to the ring plane, and in which (4n + 2) n electrons, when n is 0 or a positive integer, are associated with the ring to comply with Huckel's rule. The term "aromatic carbocyclic ring system" includes fully aromatic carbocycles and carbocycles in which at least one ring of a polycyclic ring system is 20 aromatic. The term "nonaromatic carbocyclic ring system" denotes fully saturated carbocycles as well as partially or fully unsaturated carbocycles wherein none of the rings in the ring system are aromatic. The terms "aromatic heterocyclic ring system" and "heteroaromatic ring" include fully aromatic heterocycles and heterocycles hi which at least one ring of a polycyclic ring system is aromatic. The term "nonaromatic heterocyclic ring 25 system" denotes fully saturated heterocycles as well as partially or fully unsaturated heterocycles wherein none of the rings in the ring system are aromatic. The term "aryl" denotes a carbocyclic or heterocyclic ring or ring system in which at least one ring is aromatic, and the aromatic ring provides the connection to the remainder of the molecule. The carbon moieties specified for R1 and R4 are optionally substituted. The term 30 "optionally substituted" in connection with these carbon moieties refers to carbon moieties that are unsubstituted or have at least one non-hydrogen substituent. Similarly, the term "optionally substituted" in connection with aryl and tertiary aryl refers to aryl and tertiary alkyl radicals that are unsubstituted or have a least one non-hydrogen substituent. Illustrative optional substituents include alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, 35 hydroxycarbonyl, formyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, alkoxycarbonyl, hydroxy, alkoxy, alkenyloxy, allcynyloxy, cycloalkoxy, aryloxy, alkylthio, alkenylthio, alkynylthio, cycloalkylthio, arylthio, alkylsulfinyl, alkenylsulfinyl, alkynylsulfinyl, cycloalkylsulfinyl, arylsulfinyl, alkylsulfonyl, alkenylsulfonyl, alkynylsulfonyl, cycloalkyl- WO 2006/121648 561399 PCT/US2006/016340 5 sulfonyl, arylsulfonyl, amino, alkylamino, alkenylamino, alkynylamino, arylamino, aminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkynylaminocarbonyl, aryl-aminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkynylaminocarbonyl, aryl-aminocarbonyloxy, alkoxycarbonylaniino, alkenyloxycarbony lamino, alkynyloxycarbonyl-5 amino and aryloxycarbonylamino, each further optionally substituted; and halogen, cyano and nitro. The optional further substituents are independently selected from groups lilce those illustrated above for the substituents themselves to give additional substituent radicals for R1 and R4 such as haloalkyl, haloalkenyl and haloalkoxy. As a further example, alkylamino can be further substituted with alkyl, giving dialkylamino. The substituents can 10 also be tied together by figuratively removing one or two hydrogen atoms from each of two substituents or a substituent and the supporting molecular structure and joining the radicals to produce cyclic and polycyclic structures fused or appended to the molecular structure supporting the substituents. For example, tying together adjacent hydroxy and methoxy groups attached to, for example, a phenyl ring gives a fused dioxolane structure containing 15 the linking group -0-CH2-0-. Tying together a hydroxy group and the molecular structure to which it is attached can give cyclic ethers, including epoxides. Illustrative substituents also include oxygen, which when attached to carbon forms a carbonyl function. Similarly, sulfur when attached to carbon forms a thiocarbonyl function. As referred to herein, "alkyl", used either alone or in compound words such as 20 "alkylthio" or "haloalkyl" includes straight-chain or branched alkyl, such as, methyl, ethyl, R-propyl, /-propyl, or the different butyl, pentyl or hexyl isomers. "Alkenyl" includes straight-chain or branched alkenes such as ethenyl, 1-propenyl, 2-propenyl, and the different butenyl, pentenyl and hexenyl isomers. "Alkenyl" also includes polyenes such as 1,2-propadienyl and 2,4-hexadienyl. "Alkynyl" includes straight-chain or branched alkynes 25 such as ethynyl, 1-propynyl, 2-propynyl and the different butynyl, pentynyl and hexynyl isomers. "Alkynyl" can also include moieties comprised of multiple triple bonds such as 2,5-hexadiynyl. "Alkoxy" includes, for example, methoxy, ethoxy, rc-propyloxy, isopropyloxy and the different butoxy, pentoxy and hexyloxy isomers. "Alkoxyalkyl" includes, for example, CH3OCH2, CH3OCH2CH2, CH3CH2OCH2, CH3CH2OCH2CH2. 30 "Hydroxyalkyl" includes, for example, HOCH2CH2CH2, CH3CH(OH)CH2CH25 CH3CH(OH)CH2- "Alkenyloxy" includes straight-chain- or branched alkenyloxy moieties. Examples of "alkenyloxy" include H2C=CHCH20, (CH3)2C=CHCH20, (CH3)CH=CHCH20, (CH3)CH=C(CH3)CH20 and CH2=CHCH2CH20. "Alkynyloxy" includes straight-chain or branched alkynyloxy moieties. Examples of "alkynyloxy" include 35 HC=CCH20, CH3OCCII20 and CH3C=CCH2CH20.. "Alkylthio" includes branched or straight-chain alkylthio moieties such as methylthio, ethylthio, and the different propylthio, butylthio, pentylthio and hexylthio isomers. "Alkylsulfinyl" includes both enantiomers of an alkylsulfinyl group. Examples of "alkylsulfinyl" include CH3S(0), CH3CH2S(0), WO 2006/121648 561399 PCT/US2006/016340 6 CH3CH2CH2S(0), (CH3)2CHS(0) and the different butylsulfinyl, pentylsulfinyl and hexylsulfinyl isomers. Examples of "alkylsulfonyl" include CH3S(0)2, CH3CH2S(0)2, CH3CH2CH2S(0)2, (CH3)2CHS(0)2 and the different butylsulfonyl, pentylsulfonyl and hexylsulfonyl isomers. "Alkylamino", "alkenylthio", "alkenylsulfinyl", "alkenylsulfonyl", 5 "alkynylthio", "allcynylsulfinyl", "alkynylsulfonyl", and the like, are defined analogously to the above examples. Examples of "alkylcarbonyl" include C(0)CH3, C(0)CH2CH2CH3 and C(0)CH(CH3)2. Examples of "alkoxycarbonyl" include CH30C(=0), CH3CH20C(=0), CH3CH2CH20C(=:0), (CH3)2CH0C(=0) and the different butoxy- or pentoxycarbonyl isomers. "Cycloalkyl" includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, and ■ 10 cyclohexyl. The term "cycloalkoxy" includes the same groups linked through an oxygen atom such as cyclopentyloxy and cyclohexyloxy. "Cycloalkylamino" means the amino nitrogen atom is attached to a cycloalkyl radical and a hydrogen atom and includes groups such as cyclopropylamino, cyclobutylamino, cyclopentylamino and cyclohexylamino. "(Alkyl)(cycloalkyl)amino" means a cycloalkylamino group where the amino hydrogen 15 atom is replaced by an alkyl radical; examples include groups such as (methyl)(cyclopropyl)amino, (butyl)(cyclobutyl)amino, (propyl)cyclopentylamino, (methyl) cyclohexylamino and the like. "Cycloalkenyl" includes groups such as cyclopentenyl and cyclohexenyl as well as groups with more than one double bond such as 1,3- and 1,4-cyclohexadienyl. 20 The term "halogen", either alone or in compound words such as "haloalkyl", includes fluorine, chlorine, bromine or iodine. The term "1-2 halogen" indicates that one or two of the available positions for that substituent may be halogen which are independently selected. Further, when used in compound words such as "haloalkyl", said alkyl may be partially or fully substituted with halogen atoms which may be the same or different. Examples of 25 "haloalkyl" include F3C, C1CH2, CF3CH2 and CF3CCI2. The total number of carbon atoms in a substituent group is indicated by the "Cj-Cj" prefix where i and j are, for example, numbers from 1 to 3; e.g., Cj-C3 alkyl designates methyl through propyl. Although there is no definite limit to the size of RJ and R4, optionally substituted alkyl 30 moieties of R1 commonly include 1 to 6 carbon atoms, more commonly 1 to 4 carbon atoms and most commonly 1 to 3 carbon atoms in the alkyl chain. Optionally substituted alkyl moieties of R4 commonly include 1 to 14 carbon atoms, more commonly 1 to 8 carbon atoms and most commonly 1 to 4 carbon atoms in the alkyl chain. Optionally substituted alkenyl and alkynyl moieties of R1 commonly include 2 to 6 carbon atoms, more commonly 35 2 to 4 carbon atoms and most commonly 2 to 3 carbon atoms in the alkenyl or alkynyl chain. Optionally substituted alkenyl and alkynyl moieties of R4 commonly include 2 to 14 carbon atoms, more commonly 3 to 8 carbon atoms and most commonly 3 to 4 carbon atoms in the alkenyl or alkynyl chain. WO 2006/121648 561399 PCT/US2006/016340 7 As indicated above, the carbon moieties of R1 and R4 may be an aromatic ring or ring system. Examples of aromatic rings or ring systems include a phenyl ring, 5- or 6-membered heteroaromatic rings, 3- to 8-membered saturated or unsaturated carbocyclic ring systems, aromatic 8-, 9- or 10-membered fused carbobicyclic ring systems and aromatic 8-, 9- or 10-5 membered fused heterobicyclic ring systems wherein each ring or ring system is optionally substituted. The term "optionally substituted" in connection with these R* and R4 carbon moieties refers to carbon moieties which are unsubstituted or have at least one non-hydrogen substituent. These carbon moieties may be substituted with as many optional substituents as can be accommodated by replacing a hydrogen atom with a non-hydrogen substituent on any 10 available carbon or nitrogen atom. Commonly, the number of optional substituents (when present) ranges from one to four. As used herein, the terms "comprises," "comprising," "includes," "including," "has," "having" or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a composition, process, method, article, or apparatus that comprises a list of 15 elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, process, method, article, or apparatus. Further, unless expressly stated to the contrary, "or" refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or 20 present), and both A and B are true (or present). Also, the indefinite articles "a" and "an" preceding an element or component of the invention are intended to be nonrestrictive regarding the number of instances (i.e. occurrences) of the element or component. Therefore "a" or "an" should be read to include one or at least one, and. the singular word form of the element or component also includes the 25 plural unless the number is obviously meant to be singular. Combining chemicals and adding chemicals refers to contacting the chemicals with each other. Numeric ranges are inclusive of each and every integer value defining the range. One skilled in the art also recognizes that the compounds of Formulae 1 and 4 are in 30 equilibrium with their respective tautomeric counterparts of Formulae la and 4a, as shown in Exhibit 1. WO 2006/121648 561399 PCT/US2006/016340 8 Exhibit 1 R "C02H R1 w oh •co2h 1 la O oh R1 ■CI "c02h 4 Unless expressly stated otherwise, references to Formulae 1 and 4 in the present disclosure and claims are to be construed to include all tautomers, including Formulae la and 4a, respectively. The nitrogen atom in the compounds of Formulae 1, 3, 4, 6, 7 and 8 (including la and 4a) can be protonated, allowing said compounds to form acid-addition salts with inorganic or organic acids including but not limited to hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, or 4-toluenesulfonic acids. Embodiments of the present invention include: Embodiment Al. A method as set forth in the Summary of the Invention wherein R1 is an optionally substituted carbon moiety. Embodiment A2. A method of Embodiment Al wherein R1 is optionally substituted cyclopropyl or an optionally substituted phenyl. Embodiment A3. A method of Embodiment A2 wherein R1 is optionally substituted cyclopropyl. Embodiment A4. A method of Embodiment A2 wherein R1 is optionally substituted phenyl. Embodiment A5. A method of Embodiment A3 wherein R1 is unsubstituted cyclopropyl. Embodiment A6. A method of Embodiment A4 wherein R1 is phenyl substituted at the para position and optionally substituted at other positions. WO 2006/121648 561399 PCT/US2006/016340 9 Embodiment A7. A method of Embodiment A6 wherein R1 is phenyl substituted with Br or CI at the para position and optionally substituted with 1-2 halogen at other positions. Embodiment A8. A method of Embodiment A7 wherein R1 is phenyl substituted with 5 Br or CI at the para position. Embodiment A9. A method as set forth in the Summary of the Invention wherein R4 is Cj-C]4 alkyl, C2-Cj4 alkoxyalkyl. C2-Ci4 hydroxyalkyl or benzyl. Embodiment A10. A method of Embodiment A9 wherein R4 is Cj-C^ alkyl, C2-C^4 alkoxyalkyl or C2-Ci4 hydroxyalkyl. 10 Embodiment All. A method of Embodiment A10 wherein R4 is Cr Cg allcyl, C2-Cg alkoxyalkyl or C2-C8 hydroxyalkyl. Embodhnent A12. A method of Embodiment Al 1 wherein R4 is C|-Cg alkyl or C2-Cg alkoxyalkyl. Embodiment A13. A method of Embodiment. A12 wherein R4 is CJ-C4 alkyl. 15 Embodiment Bl. A method as set forth in the Summary of the Invention wherein the alkanol is methanol or ethanol. Embodiment B2. A method of Embodiment Bl wherein the alkanol is ethanol. Embodiment B3. A method as set forth in the Summary of the Invention wherein the volume ratio of the first portion of water to the compound of Formula 2a ranges 20 from about 10 to about 0.01. Embodiment B4. A method of Embodiment B3 wherein the volume ratio of the first portion of water to the compound of Formula 2a ranges from about 6 to about 1. Embodiment B5. A method of Embodiment B4 wherein the volume ratio of the first portion of water to the compound of Formula 2a ranges from about 3 to about 2. 25 Embodiment B6. A method as set forth in the Summary of the Invention wherein the volume ratio of the first portion of water to the alkanol ranges from about 0.01 to about 100. Embodiment B7. A method of Embodiment B6 wherein the volume ratio of the first portion of water to the alkanol ranges from about 1 to about 50. 30 Embodiment B8. A method of Embodiment B7 wherein the volume ratio of the first portion of water to the alkanol ranges from about 5 to about 10. Embodiment B9. A method as set forth in the Summary of the Invention wherein the first base is an alkali metal hydroxide. Embodiment B10. A method of Embodiment B9 wherein the alkali metal hydroxide is 3 5 sodium, hydroxide or potassium hydroxide. Embodiment Bl 1. A method of Embodiment B10 wherein the alkali metal hydroxide is sodium hydroxide. WO 2006/121648 561399 PCT/US2006/016340 Embodiment B12. A method of Embodiment B9 wherein the molar ratio of the first base to the compound of Formula 2a ranges from about 0.5 to about 2. Embodiment B13. A method of Embodiment B12 wherein the molar ratio of the first base to the compound of Formula 2a ranges from about 0.7 to about 1.5. 5 Embodiment B14. A method of Embodiment B13 wherein the molar ratio of the first base to the compound of Formula 2a is in a range of about 0.9 to about 1.2. Embodiment B15. A method as set forth in the Summary of the Invention wherein the pH of the first resultant solution is in a range of about 11 to about 13. Embodiment B16. A method as set forth in the Summary of the Invention wherein step 10 (1) is conducted at a temperature in a range of about 5 to about 40 °C. Embodiment B17. A method of Embodiment B16 wherein the temperature is in a range of about 20 to about 30 DC. Embodiment CI. A method as set forth in the Summary of the Invention wherein the first resultant solution comprising the compound of Formula 2b is contacted with 15 the compound of Formula 3 or an acid salt thereof. Embodiment C2. A method as set forth in the Summary of the Invention wherein the molar ratio of the compound of Formula 3 or an acid salt thereof to the compound of Formula 2a is in a range of about 0.6 to about 1.2. Embodiment C3. A method of Embodiment C2 wherein the molar ratio of the 20 compound of Formula 3 or an acid salt thereof to the compound of Formula 2a is in a range of about 0.6 to about 1.0. Embodiment C4. A method of Embodiment C3 wherein the molar ratio of the compound of Formula 3 or an acid salt thereof to the compound of Formula 2a is in a range of about 0.7 to about 0.9. 25 Embodiment C5. A method as set forth in the Summary of the Invention wherein the second base is an alkali metal hydroxide. Embodiment C6. A method of Embodiment C5 wherein the alkali metal hydroxide is sodium hydroxide or potassium hydroxide. Embodiment C7. A method of Embodiment C6 wherein the alkali metal hydroxide is 30 sodium hydroxide. Embodiment C8. A method of Embodiment C5 wherein the molar ratio of the second base to the compound of Formula 3 is in a range of about 2 to about 0.5. Embodiment C9. A method of Embodiment C8 wherein the molar ratio of the second base to the compound of Formula 3 is in a range of about 1.2 to about 0.8. 35 Embodiment C10. A method as set forth in the Summary of the Invention wherein the the pH of the second resultant solution is in a range of about 9 to about 12. Embodiment CI 1. A method of Embodiment C10 wherein the pH ranges from about 10.5 to about 11.5. WO 2006/121648 561399 PCT/US2006/016340 11 Embodiment C12. A method as set forth in the Summary of the Invention wherein step (2) is conducted at a first temperature in a range of about 0 to about 40 °C, and later increased to a second temperature in a range of about 10 to about 70 °C. Embodiment CI 3. A method of Embodiment C12 wherein the first temperature is in a 5 range of about 20 to about 40 °C, and the second temperature is in a range of about 50 to about 65 °C. Embodiment Dl. A method as set forth in the Summary of the Invention wherein the acid added in step (3) is a mineral acid. Embodiment D2. A method of Embodiment Dl wherein the acid is sulfuric acid or 10 hydrochloric acid. Embodiment D3. A method as set forth in the Summary of the Invention wherein after the addition of the acid in step (3), the second resulting solution has a pH in a range of below about 3. Embodiment D4. A method of Embodiment D3 wherein the pH is in a range of about 1 15 to about 2. Embodiment D5. A method as set forth in the Summary of the Invention wherein step (3) is conducted at a first temperature in a range of about 30 to about 55 °C, and later decreased to a second temperature in a range of about 0 to about 20 °C. Embodiment D6. A method of Embodiment D5 wherein the first temperature is in a 20 range of about 40 to about 45 °C, and the second temperature is in a range of about 0 to about 10 °C. Embodiment El. A method as set forth in the Summary of the Invention preparing the compound of Formula 4 wherein the chlorinating agent is selected from the group consisting of chlorine, hypochlorous acid, sulfuryl chloride, sodium 25 hypochlorite, calcium hypochlorite and potassium hypochlorite. Embodiment E2. A method as set forth in the Summary of the Invention preparing the compound of Formula 6 wherein the chloride displacement agent is selected from the group consisting of phosphorus oxychloride, thionyl chloride, oxalyl chloride, phosgene, diphosgene and triphosgene. 30 In the following Schemes 1-6 the definitions of R1, R2, R3 and R4 in the compounds of Formulae X through 8 are as defined above in the Summary of the Invention and description of Embodiments unless otherwise indicated. The present method for preparing optionally 2-substituted l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid compounds of Formula 1 is illustrated in Schemes 1 and 2. As 35 shown in Scheme 1, in the first step a mixture comprising an oxalacetate diester salt of Formula 2a, a lower alkanol (i.e. C4-C4 alkanol) and water is combined with a solution comprising a base dissolved in water. The base is present in sufficient amount such that the WO 2006/121648 561399 PCT/US2006/016340 12 resulting solution comprising the salt of Formula 2b has a pH ranging from about 10.to about 14. In this pH range the ester group geminal to the OM on Formula 2a is believed to be selectively saponified to form the corresponding C02M group of Formula 2b. Scheme 1 R202C> . n C02R base 0M H20 OM 2a 2b wherein M is alkali metal and R2 and R3 are independently Cj-C4 alkyl. Typically the mixture comprising an oxalacetate diester salt of Formula 2a, Cj-C4 alkanol and water is formed by adding the salt of Formula 2a to a mixture of the C1-C4 10 alkanol and water, but other orders of addition are possible. Furthermore the oxalacetate diester salt of Formula 2a can be prepared in situ by combining the corresponding oxalacetate diester with the alkanol and/or water containing about one equivalent of sodium or potassium hydroxide or alkoxide. The mixture comprising the oxalacetate diester salt of Formula 2a, C1-C4 alkanol and water is typically present as a solution wherein the 15 oxalacetate diester salt is Formula 2a is entirely dissolved but depending on amounts of alkanol and water can also be a suspension wherein some of the oxalacetate diester salt of Formula 2a remains undissolved. While the potassium salt of Formula 2a works satisfactorily for this method, the sodium salt is preferred, as it is conveniently prepared in excellent yield. Although a wide range of carbon-bearing moieties can be used as R2 and 20 R3, for reason of cost and convenience, lower alkyl (i.e. C1-C4 alkyl) groups, i.e. methyl, ethyl, ra-propyl, isopropyl, n-butyL sec-butyl or /erf-butyl, are most satisfactory, and short alkyl groups such as ethyl work well. The Cr C4 alkanol is selected from the possible C^-C4 alkanols, i.e. methanol, ethanol, n-propanol, isopropanol, w-butanol, sec-butanol, tert-butanol, and their mixtures. 25 Ethanol, optionally containing denaturing alcohols such as isopropanol, has been found to work well for this reaction, but other C1-C4 alkanols such as methanol can be used. As the mixture comprises water, ethanol can be conveniently used as its 95 % ethanol -5 % water azeotrope. Typically the volume ratio of the water to the compound of Formula 2 a in the mixture before addition of the base ranges from about 0.01 to about 10, more typically from 30 about 1 to about 6, and most typically from about 2 to, about 3. Most typically the volume ratio of the water-alkanol mixture to the compound of Formula 2a in the mixture before addition of the base ranges from about 2 to about 6. Typically the volume ratio of the water to the alkanol in the mixture before addition of the base ranges from about 0.01 to about 100, more typically from about 1 to about 50, and most typically from about 5 to about 10. When WO 2006/121648 561399 PCT/US2006/016340 13 ethanol is used as the C-1-C4 alkanol, about 2.5 volumes of a mixture of about 15 wt % ethanol in water relative to the compound of Formula 2a works well. The mixture comprising the oxalacetate diester salt of Formula 2a, Cj C4 alkanol and water is combined with a solution of a base in water. Preferably the aqueous solution of the 5 base is added to the mixture comprising oxalacetate diester salt of Formula 2a, C1-C4 alkanol and water, as this order of addition prevents the compound of Formula 2a from being temporarily exposed to excessive base. The base needs to be strong enough to provide a pH in the range of about 10 to 14. Most conveniently and inexpensively the base is an alkali metal hydroxide, such as sodium or potassium hydroxide. Typically about 0.5 to about 2, 10 more typically about 0.7 to about 1.5, and most typically about 0.9 to 1.2 molar equivalents of the base is used relative to the compound of Formula 2a. This amount of base is believed to saponify the compound of Formula 2a to form the compound of Formula 2b while providing a final pH in the range of about 10 to 14. Preferably the amount of base is selected so that the final pH is in the range between about 11 and 13. 15 The base is added as a water solution to the mixture comprising the oxalacetate diester salt of Formula 2a, C1-C4 alkanol and water. Typically the water solution of the base comprises about 1 to 50 wt % of base, more typically about 10 to 40 wt .% of base, and most typically about 20 to 30 wt % of base. During the addition of the aqueous base solution the temperature of the reaction mixture is typically maintained between about 5 and 40 °C, and 20 more typically about 20 to 30 °C (e.g., about 25 °C). The method of Scheme 1 forms a hydrolysate mixture containing predominately the monoalkyl oxalacetate salt compound of Formula 2b, generally in the form of a solution. This solution is typically used directly in unrefined form in the next step. Although the intermediate monoalkyl oxalacetate salt compound of Formula 2b is typically not isolated, 25 based on the high yields for the overall method, yields of the compound of Formula 2b from the step shown as Scheme 1 are reasonably believed to be on the order of 80 to 90 %. As shown in Scheme 2, in the next step the compound of Formula 1 is prepared by contacting the hydrolysate mixture comprising the compound of Formula 2b formed in the first step with a carboximidamide of Formula 3. 30 - Scheme 2 O 2b + NH 2. acidify 1. pH 9-12 3 1 Typically about 0.6 to about 1.2, more typically about 0.6 to about' 1, most typically about 0.7 to about 0.9 molar equivalents of the carboximidamide of Formula 3 is employed WO 2006/121648 561399 PCT/US2006/016340 14 relative to the dialkyl ester of Formula 2a used to prepare the intermediate compound of Formula 2b. The carboximidamide of Formula 3 can be either in the form of its free base or in the form of a salt such as its hydrochloride salt. Although the hydrolysate mixture can be added to the carboximidamide of Formula 3, typically the carboximidamide is added to the 5 hydrolysate mixture. The carboximidamide can be contacted directly with the hydrolysate mixture, or it can be added as a solution in a suitable solvent, such as water or a lower alkanol. Typically the carboximidamide of Formula 3 is contacted with the hydrolysate mixture at a temperature between about 0 and about 40 °C, more typically between about 20 to about 10 40 °C, preferably between about 20 to about 30 °C. As is discussed below, the temperature is often subsequently raised to accelerate completion of the reaction. For this reaction step the solution formed needs to have a pH in the range from about 9 to about 12, preferably about 10 to about 12, more preferably about 10.5 to about 11.5. A sufficient amount of base is thus added to provide this pH range. If the carboximidamide of 15 Formula 3 is used in the form of its free base, the amount of additional base needed to achieve the range of about 9 to 12 can be zero. However, if the carboximidamide of Formula 3 is in the form of a salt, such as its hydrochloride salt, a sufficient amount of base is needed to provide the needed pH range. Although the base can added to the carboximidamide salt or a solution thereof before adding the carboximidamide to the 20 hydrolysate mixture, or the base can be added to the hydrolysate mixture before adding the carboximidamide salt, preferably the base is added to the hydrolysate mixture after addition of the carboximidamide salt. The base needs to be sufficiently strong to provide the needed pPI; an alkali metal hydroxide such as sodium or potassium hydroxide works well for this purpose. When the carboximidamide of Formula 3 is in the form of a salt, the molar 25 equivalents of the base relative to the carboximidamide is typically in the range of about 0.5 to about 2, and more typically in the range of about 0.8 to about 1.2. Typically the base is dissolved in a solvent such as water before addition to the reaction mixture. After the carboximidamide of Formula 3 is combined with the hydrolysate mixture together with an amount of base needed to provide a pH range of about 9 to 12 in the 30 reaction mixture, the reaction mixture is often warmed to accelerate completion of the reaction. For this purpose the temperature is typically adjusted to about 10 to about 70 °C, and more typically to about 50 to about 65 °C. The reaction forms the compound of Formula 1 as its carboxylate salt, which generally is dissolved in the .reaction mixture. To isolate the compound of Formula 1, the reaction 35 mixture is typically cooled to a temperature of about 55 °C or lower (e.g., between about 30 and 55 °C, often conveniently about 45 °C), and an acid is added to acidify the reaction mixture and convert the compound of Formula 1 from its carboxylate salt to its free acid form. The usual common mineral acids such as hydrochloric acid, sulfuric acid or WO 2006/121648 561399 PCT/US2006/016340 15 phosphoric acid work well. The acid is added in sufficient amount to lower the pH of the reaction mixture below about 3, typically in the range of about 1 to about 2. Often under these conditions the product of Formula 1 will crystallize. The reaction mixture is then preferably cooled to the range of about 0 to about 10 °C to promote crystallization, and the 5 solid product is collected by filtration, washing and drying. If the product of Formula 1 does not form a solid, it can be isolated by extracting the reaction mixture with a suitable water-immiscible solvent such as ether, dichloromethane or ethyl acetate, drying, and evaporating the solvent. The method of Schemes 1 and 2 is illustrated in Step B of Example 1. The 10 carboximidamide compounds of Formula 3 can be prepared by methods known in the art, including the improved modifications taught in U.S. Patents 4,323,570 and 4,012,506. The preparation of a compound of Formula 3 is illustrated in Step A of Example 1. Thus l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid compounds of Formula 1 can be conveniently prepared in good yield from compounds of Formula 2a and 3 according to the 15 aforedescribed method. The l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid compounds of Formula 1 prepared by this method can then be transformed using further reaction steps into a variety of optionally substituted 4-pyrimidinecarboxylic acids and esters. The first subsequent reaction, shown in Scheme 3, prepares a compound of Formula 4 by contacting the compound of Formula 1 with a chlorinating agent. 20 Scheme 3 O X CI Chlorinating agent HN rr^ 1 Al R1 N C02H 4 This method involves the replacement of the hydrogen at the 4-position on the l,6-dihydro-6-oxo-4-pyrimidinyl ring with chlorine. As is known in the art, a variety of chlorinating agents (i.e. reagents that replace hydrogen atoms in organic molecules with 25 chlorine) can be used for this type of transformation. Described below are illustrative procedures for the method when the chlorinating agent is chlorine, hypochlorous acid, sulfuryl chloride or inorganic hypochlorite such as sodium hypochlorite, calcium hypochlorite and potassium hypochlorite. In one procedure, a compound of Formula 1 is suspended in an inert solvent, typically 30 about 3 to 6 volumes of water, optionally containing 0.5 to 3.5 molar equivalents of mineral acid, preferably hydrochloric acid. About 0.95 to about 1.2 molar equivalents of a chlorinating agent, preferably chlorine or hypochlorous acid (HOC1), is added with good agitation at about 10 to about 35 °C. If hypochlorous acid is used, it can be generated in situ WO 2006/121648 561399 PCT/US2006/016340 16 by adding at least 1 molar equivalent of mineral acid to the suspension of the compound of Formula 1 prior to adding an inorganic hypochlorite, preferably sodium hypochlorite (NaOCl) as typically a 5 to 14 % aqueous solution. Excess chlorinating agent can be removed by purging with an inert gas or by adding a reducing agent such as sodium sulfite. 5 If the product of Formula 4 forms a solid, it can be isolated by filtration. If the product of Formula 4 does not form a solid, it can be isolated by extraction of the aqueous reaction mixture with a water-immiscible solvent, such as ether, dichloromethane or ethyl acetate, drying, and evaporating the extraction solvent. This procedure is illustrated in Step CI of Example 1. 10 In another procedure, the compound of Formula 1 is dissolved in an inert solvent, preferably about 1.5 to about 4 volumes of water, optionally containing about 0 to 3.5 molar equivalents of inorganic base, preferably sodium hydroxide or potassium hydroxide. About 0.95 to about 1.2 molar equivalents of a chlorinating agent, preferably chlorine or sodium hypochlorite (NaOCl, typically as a 5 to 14 % aqueous solution), is added with good 15 agitation to the reaction mixture at about 0 to 70 °C, typically about 10 to 35 °C. When sodium hypochlorite is used as chlorinating agent, the amount of base is preferably about 0.85 to 1.2 molar equivalents relative to the compound of Formula 1. Excess chlorinating agent can be removed by purging with an inert gas or by adding a reducing agent such as sodium sulfite. The reaction mixture is then acidified by adding a mineral acid, such as 20 concentrated hydrochloric acid, to lower the pH to about 0.5 to 3 and produce the free acid form of the compound of Formula 4. If the product of Formula 4 is a solid, it can be isolated by filtering. If the product of Formula 4 is not a solid, it can be isolated by extraction of the aqueous reaction mixture with a water-immiscible solvent, such as ether, dichloromethane or ethyl acetate, drying, and evaporating the extraction solvent. This procedure is illustrated in 25 Step C2 of Example 1. The second subsequent reaction, shown in Scheme 4, prepares a compound of Formula 6 by contacting the compound of Formula 4 with a chloride displacement agent. Scheme 4 CI " [hydrolysis] R1 N X02H 6 30 This method involves the replacement of the 6-oxo function on the l,6-dihydro-6-oxo- 4-pyrimidinyl ring with chlorine. As is known in the art, a'variety of chloride displacement agents (i.e. reagents that replace hydroxy moieties in organic molecules with chlorine) can Chloride displacement agent 4 >■ CI WO 2006/121648 561399 PCT/US2006/016340 17 be used for this type of transformation. As the hydroxyl moiety on the carboxylic acid function can also be replaced by chlorine, contact with chloride displacement agents often result in formation of intermediate acyl chlorides of Formula 5, wherein R1 is H or an optionally substituted carbon moiety, which are hydrolyzed on contact with water during 5 reaction work up to provide the compounds of Formula 6. Described below are illustrative procedures for the method when the chloride displacement agent is phosphorus oxychloride, thionyl chloride, oxalyl chloride, phosgene, diphosgene or triphosgene. In one procedure, a compound of Formula 4 is combined with about 2 to about 4 molar equivalents of chloride displacement agent such as phosphorus oxychloride. Optionally 10 about 0.05 to 1.0 molar equivalents of A^,iV-dimethylformamide (DMF), typically without added solvent, is also included in the reaction mixture. The reaction mixture is maintained at a temperature between about 10 and about 100 °C, typically between about 70 and about 95 °C. Excess phosphorus oxychloride can be conveniently removed by distillation at a pressure of about 6 to 30 kPa. The reaction mixture (believed to consist of the acid chloride 15 intermediate of Formula 5 and polymeric chlorophosphoric acids) is then carefully added to water optionally containing about 20 to 40 % of a water-miscible organic co-solvent, preferably tert-butanol. About 25 wt % of ferf-butanol in the mixture works well. If the product of Formula 6 is a solid, the resulting mixture can be further diluted with water to promote crystallization. The suspension of the crystalline product of Formula 6 is then 20 filtered, washed with water, and typically dried. If the product of Formula 6 does not form a solid, it can be isolated by extracting the reaction mixture with a suitable water-immiscible solvent such as ether, dichloromethane or ethyl acetate and drying the solution. The solvent can be evaporated to isolate the compound of Formula 6, or if the solvent is suitable for the next reaction, the solution can be used directly. This procedure is illustrated in Step Dl of 25 Example 1. In another procedure, a compound of Formula 4 is mixed with about 2 to 4 volumes of an aprotic organic solvent, such as ethyl acetate, tetrahydrofuran or 1,2-dichloroethane, optionally about 0.02 to 0.2 molar equivalents of iV^-dimethylformamide, and about 2.0 to about 3.0 molar equivalents of a chloride displacement agent, preferably thionyl chloride, 30 oxalyl chloride or phosgene. The reaction mixture is maintained at typically about 20 to 100 °C, preferably at about 50 to 70 °C, for typically 2 to 12 h. The reaction mixture (believed to consist of the acid chloride intermediate of Formula 5) is then carefully added to water with agitation. The product of Formula 6 can be isolated or a solution formed as described for the first procedure. The present procedure is illustrated in Step D2 of 35 Example 1. The third subsequent reaction, shown in Scheme 5, prepares a compound of Formula 7 by contacting the compound of Formula 6 with ammonia. WO 2006/121648 561399 PCT/US2006/016340 18 Scheme 5 nh2 nh3 €1 6 R1 N c02h 7 10 15 20 This method involves the replacement of the chlorine at the 6-position on the pyrimidinyl ring with an amino function. As is known in the art, this type of transformation generally involves contact of 6-chloropyrimidine compounds with ammonia. Typically the ammonia is provided from a supply cylinder or as a concentrated solution in a solvent (e.g., ammonium hydroxide), although ammonia can also be formed in situ by contact of ammonium salts such as ammonium chloride or ammonium sulfate with bases. Described below is an illustrative procedure. hi this procedure, a compound of Formula 6 is mixed with ammonia in a solvent. Although only about 1 molar equivalent of ammonia is stoichiometrically needed if another base is present, typically ammonia is the only base present and 3 to 7 molar equivalents of ammonia are used to obtain a rapid reaction rate. A wide variety of inert solvents can be used, including water, alkanols such as ethanol, and ethers such as tetrahydrofuran; water is inexpensive and often works well. The reaction mixture is maintained at a temperature in the range of about 0 to 100 °C, typically about 80 to 90 °C, and at a pressure typically in the range of about 100 (i.e. atmospheric pressure) to about 500 kPa. Under these conditions the reaction is typically complete in about 1 to 5 h. The product of Formula 7 can be isolated by cooling the mixture, optionally venting excess pressure, distilling to remove excess ammonia and solvent, adding 1 to 2 molar equivalents of mineral acid, preferably aqueous hydrochloric acid, to lower the pH of about 2. If the product of Formula 7 forms solid, it can be collected by filtration, washed with water and dried. If the product of Formula 7 does not form a solid, it can be isolated by extracting the reaction mixture with a suitable water-immiscible solvent such as ether, dichloromethane or ethyl acetate, drying, and evaporating the solvent. This procedure is illustrated in Step E of Example 1. The fourth subsequent reaction, shown in Scheme 6, prepares a compound of Formula 8 by contacting the compound of Formula 7 with an R4 transfer agent. WO 2006/121648 561399 PCT/US2006/016340 19 Scheme 6 nh2 R4 transfer agent 7 R1 N' 'co2r4 8 wherein R4 is an optionally substituted carbon moiety. This method involves conversion of the carboxylic acid group (C02H) on the 5 compound of Formula 7 to the corresponding ester group (C02R4) 011 the compound of transformations in organic chemistry, and an enormous variety of procedures are known. For reviews, see for example, C. A. Buehler and D. E. Pearson, Survey of Organic Syntheses, Wiley-Interscience, New York, 1970, pp. 802-827. Most direct procedures involve 10 contacting carboxylic acids with alcohols (e.g., R4OH) in the presence of an acid catalyst or a dehydrating coupling agent, or contacting with compounds providing the alcohol moiety and also consuming the water formed (e.g., orthoesters, carbonates) also typically in the presence of an acid catalyst, or contacting carboxylic acids in the presence of a base with alkylating agent-type chemical compounds in which the R4 radical is bonded to a nucleofuge 15 (e.g., R4X wherein X is a nucleophilic reaction leaving group, also known as a nucleofuge). Such dehydrating coupling agents as dicyclohexyl carbodiimide, N-{ 3-dimethylaminopropyl)-iV'-ethylcarbodiimide, 1-propanephosphonic acid cyclic anhydride and carbonyl diimidazole are well known in the art, but in view of their cost and the potential interference of the amino group, acid catalysis is the preferred means of preparing 20 compounds of Formula 8 from compounds of Formula 7 and alcohols of formula R4OH. In the method of Scheme 6 compounds such as alcohols of formula R4OH, orthoesters (e.g., (R40)3CRa wherein Ra is H, OR4 or an optionally substituted carbon moiety), carbonates (e.g., R40C(0)0R4) and compounds of formula R4X are R4 transfer agents, as they provide the R4 moiety needed for transforming the carboxylic acid group of the compound of 25 Formula 7 to the ester group of the compound of Formula 8. As defined in the present disclosure and claims, "R4 transfer agent" means a chemical compound capable of transferring the radical R4 to a carboxylic acid group (i.e. C02H) or derived carboxylate acid anion (i.e. C02e) to form the corresponding ester (i.e. C02R4). Acid-catalyzed reaction of alcohols of formula R4OH and corresponding orthoesters of formula (R40)3CRa and 30 carbonates of formula R40C(0)0R4 as the R4 transfer agent work best when they are liquid at the reaction temperature and of comparatively moderate molecular complexity and size (e.g., molecular weights less than 200, preferably less than 150). Reaction with R4X as the Formula 8. Conversion of carboxylic acids to esters is one of the oldest known WO 2006/121648 561399 PCT/US2006/016340 20 R4 transfer agent works well for R4 groups of both small and large structural size and complexity. Described below are illustrative procedures for this method. In a procedure using an alcohol of formula R4OH as the R4 transfer agent with an acid catalyst, a compound of Formula 7 is mixed with typically about 2 to 10 volumes of the 5 alcohol of formula R4OH and a strong acid as a catalyst. Strong protic acids have a pKa of less than 3. Examples of useful strong protic acids include phosphoric acid, sulfuric acid, hydrogen chloride, trifluoroacetic acid, j9-toluenesulfonic acid, camphorsulfonic acid, methanesulfonic acid and trifluoromethanesulfonic acid. The acids is preferably concentrated and contain as little water as feasible. Hydrogen chloride can be 10 advantageously generated by adding thionyl chloride to the alcohol. Useful strong protic acids also include solid catalysts such as sulfonated polystyrene and perfluorinated ion-exchange resins such as Nafion®. Concentrated sulfuric acid is an inexpensive acid that works well for this method. Besides protic acids, a Lewis acid such as boron trifluoride (e.g., BF3 etherate) can be used as the strong acid. Typically about 2 to 4 molar equivalents 15 of the acid is used relative to the compound of Formula 7, but lesser or greater amounts can be used. The acid is typically added to the reaction mixture last. Addition of the acid can be highly exothermic, so cooling of the reaction mixture may be needed to maintain the desired reaction temperature and prevent excessive boiling of the alcohol. Typically the reaction mixture ,is maintained at a temperature of about 20 to 100 °C, often around 70 °C. Under 20 these conditions the reaction typically reaches maximum conversion in about 2 to 24 h. The reaction can be accelerated and higher conversions to the ester achieved by distilling out the water that is produced; adding more alcohol and/or acid catalyst may be desirable to compensate for any distilled out the reaction mixture along with the water. At the completion of the reaction the mixture can be concentrated to remove most of the alcohol 25 (R4OH) if it has a sufficiently low boiling point. Such concentration can also remove volatile acids such as hydrogen chloride. Polymeric acid catalysts can be removed by filtration. The reaction mixture is typically cooled to about 0 to 35 °C and diluted with water, typically 4 to 8 volumes. The pH is typically adjusted in about 5 to 10, most typically around 7, by adding bases (e.g., alkyl metal and alkaline earth metal hydroxides and 30 carbonates such as sodium hydroxide, calcium hydroxide and sodium carbonate) and also acids (e.g., acetic acid, hydrochloric acid, sulfuric acid) if needed to titrate to a particular pH. If the product of Formula 8 forms a solid, it can be isolated by filtration, washing and drying. If the product of Formula 8 does not form a solid, it can be isolated by extraction with a water-immiscible solvent such as ether, dichloromethane or ethyl acetate, drying the solution 35 and evaporating the solvent. Unreacted starting compound of Formula 7 can often be recovered by acidifying the aqueous mixture to about pH 2 and concentrating the mixture to cause separation of the compound of Formula 7. This procedure is illustrated in Step F1 of Example 1. WO 2006/121648 561399 PCT/US2006/016340 21 In a procedure using an orthoester of formula (R40)3CRa or a carbonate of formula R40C(0)0R4 as the R4 transfer agent, a strong acid is also typically used as a catalyst. The most common orthoesters are orthoformates (i.e. Ra is H) and orthoacetates (i.e. Ra is CH3). At least one molar equivalent of the orthoester of formula (R40)3CRa or carbonate of 5 formula R40C(0)0R4 is stoichiometrically needed relative to the carboxylic acid of Formula. 7 to prepare the ester in the absence of other R4 transfer agents, but about 2 to 8 molar equivalents are typically used to rapidly achieve high yields of ester and to serve as a solvent. Other solvents can also be included in the reaction mixture, such as ethers like tetrahydrofuran andp-dioxane and alcohols of formula R4OH, which can also function as R4 10 transfer agents under the reaction conditions. If an additional solvent is included in the reaction mixture, it is typically present in up to about 10 volumes relative to the compound of Formula 7. Generally the same acids useful for esterification with alcohols are also useful for esterification with orthoesters and carbonates. Typically about 2 to 4 molar equivalents of the acid is used relative to the compound of Formula 7, but lesser or greater amounts can 15 be used. The acid is typically added to the reaction mixture last Cooling may be needed during addition of the acid to prevent excessive temperatures. The reaction mixture is typically maintained at a temperature between about 20 and 100 °C, most typically between about 70 to 80 °C. Under these conditions the reaction is typically complete in about 4 to 24 h. If boiling points allow, excess orthoester, carbonate, alcohol and/or acid catalyst can 20 be removed by distillation or evaporation to give a concentrated residue. The reaction mixture can be worked up and the ester product of Formula 8 isolated using techniques similar to those described for the preceding procedure using an alcohol of formula R4OH as the R4 transfer agent. This procedure is illustrated in Step F2 of Example 1. In a procedure using a compound of formula R4X as the R4 transfer agent, X is a 25 nucleofuge. Compounds of formula R4X are frequently referred to as alkylating agents although R4 can be optionally substituted carbon moieties besides alkyl. Typically X is the conjugate base of an acid. Common nucleofuges include halogen (e.g., CI, Br, I), sulfates such as 0S(0)20R4, and sulfonates such as 0S(0)2CH3 (methanesulfonate), 0S(0)2CF3, 0S(0)2Ph-p-CH3 (p-toluenesulfonate). However, nucleofuges useful for forming esters also 30 include pyrocarbonates, silicates and phosphonates. Nucleofuges also include ethers (e.g., R4OR4) when the R4 transfer agent is an oxonium salt (e.g., 0(R4)3® BF4e). The compound of Formula 7 is contacted with the compound of formula R4X typically in a polar solvent such as acetone, acetonitrile or dimethyl sulfoxide (DMSO) and in the presence of a base. Typically about 1 to 2 equivalents each of the compound of formula R4X and the base 35 are used relative to the compound of Formula 7. Suitable bases include organic amines such as tributylamine and iV^V-diisopropylethylamine and inorganic bases such as alkali and alkaline earth metal carbonates, oxides, hydroxides and phosphates (e.g., Na2C03, K2CO3, LiOH, Li20, NaOH, KOH, Na3P04, K3PO4). The base and the compound of formula R4X WO 2006/121648 561399 PCT/US2006/016340 22 can be added either sequentially or simultaneously. Typically the reaction mixture is maintained at a temperature between about 0 and 120 °C, more typically between about 10 and 80 °C. Maintaining good agitation is important particularly if the base is an inorganic base not readily soluble in the reaction solvent. The rate of reaction can vary substantially 5 depending upon conditions, but typically the reaction is complete in about 1 to 24 h. To work up the reaction mixture, excess solvent, R4X and/or base can be removed by evaporation under reduced pressure or distillation, and excess base can be neutralized or removed by extraction with acid. If the compound of Formula 8 is a solid, dilution of the reaction mixture with water (e.g., about 4 to 10 volumes) often results in crystallization of 10 the Formula 8 compound, which can then be collected under filtration, washed and dried. If the compound of Formula 8 does not crystallize from the aqueous mixture, it be extracted using a water-immiscible solvent such as ether, dichloromethane or ethyl acetate, the solution dried, and the solvent evaporated to leave the compound of Formula 8. This procedure is illustrated in Step F3 of Example 1. 15 Compounds of Formulae 7 and 8 have been reported to have biological utility. In particular, PCT Patent Publication WO 2005/063721 discloses compounds of Formulae 7 and 8 wherein R1 is, for example, cyclopropyl or phenyl substituted with Br or CI at the phenyl para position, and R4 is, for example, Cj-C14 alkyl, C2-C14 alkoxyalkyl, C2-C14 hydroxyalkyl or benzyl, as being useful as herbicides. 20 Without further elaboration, it is believed that one skilled in the art using the preceding description can utilize the present invention to its fullest extent. The following Examples are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Steps in the following Examples illustrate a procedure for each step in an overall synthetic transformation, and the starting material for each step 25 may not have necessarily been prepared by a particular preparative run whose procedure is described in other Examples or Steps. 1H NMR and 13CNMR spectra are reported in ppm downfield from tetramethylsilane; "s" means singlet, "m" means multiplet, "br s" means broad singlet. EXAMPLE 1 30 Preparation of methyl 6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylate Step A: Preparation of cyclopropanecarboximidamide monohydrochloride A 1-L reactor equipped with a thermocouple, subsurface gas feed line, hydrogen chloride cylinder, cylinder balance and nitrogen bubbler was flushed with nitrogen and charged with cyclopropanecarbonitrile (100 g, 1.5 mol), methanol (48 g, 1.5 mol) and 35 toluene (400 mL). The reaction mixture was maintained at 15 °C under slight nitrogen positive pressure while feeding anhydrous hydrogen chloride (57 g, 1.55 mol) below the reaction mixture surface over 2 h. Then the reaction mixture was stirred for 16 h at 23 °C. WO 2006/121648 561399 PCT/US2006/016340 23 Excess hydrogen chloride was purged by bubbling nitrogen below the reaction mixture surface and venting the effluent gas through a water scrubber over 2 h. The mixture was cooled to 5 °C, and then a solution of ammonia in methanol (240 mL of a 7 M solution, 1.7 mol) was added over 10 minutes while maintaining the temperature below 25 °C. After 5 being allowed to stand an additional 1 h, the reaction mixture was distilled at reduced pressure to remove the excess methanol. The product was filtered, washed with toluene (100 mL), and suction-dried to give 170 g (94 % yield) of the title compound as a solid. NMR (DMSO-J6) 8 8.8 (br s, 4H), 1.84 (m, 1H), 1.1 (m, 4H). Step B: Preparation of 2-cyclopropyl-l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid 10 A 500-mL jacketed reactor equipped with a pH meter, temperature probe and metering addition funnel was charged with denatured ethanol (contained 5 % 2-propanol, 30 mL) and water (150 mL). The reaction mixture was stirred while diethyl oxalacetate, sodium salt (70 g, 0.33 mol) was added over 10 minutes. A solution of 25 % aqueous NaOH (14 g, 56 mL, 0.35 mol) was metered into the stirring vortex over 1 h while maintaining the 15 temperature in a range of 25 to 30 °C. The reaction mixture was stirred for an additional 30 minutes at 30 °C, and cyclopropanecarboximidamide monohydrochloride (32 wt % solution in water, 32 g, 0.267 mol) was added. A solution of 25 % aqueous NaOH (31 g, 0.19 mol) was added at a temperature ranging from 30 to 35 °C over about 1 h so as to maintain the pH in the range of 10.5-11.5. Then the resulting orange mixture was gradually heated to 60 °C 20 over a period of 1 h and held at the same temperature for additional 30 minutes. The reaction mixture was cooled to 45-50 °C, and hydrochloric acid (37 wt. % in water, 50 mL, 0.60 mol) was added over 1 h at about 45 °C (CAUTION: foaming) until the pH reached to about 1.5. The reaction mixture was cooled to 5 °C and filtered. The resulting wet cake was washed with water (3 x 20 mL), suction-dried, and dried in a vacuum-oven at 70 °C for 16 h 25 to afford 42 g (85 % yield) of the title compound as a beige solid (97 % purity by HPLC assay) decomposing at 235-236 °C. iHNMR (DMSO-J6) 5 6.58 (s, 1H), 1.95 (m, 1H), 1.0 (m, 4H). 13CNMR(DMSO-J6)8 169.2,169.0, 157.3,116.8, 17.7, 14.1. Step CI: Preparation of 5-chloro-2-cyclopropyl-l,6-dihydro-6-oxo-4-pyrimidine-30 carboxylic acid A 2-L Morton flask with overhead stirrer, thermocouple and addition funnel was charged with 2-cyclopropyl-l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (161 g, 0.90 mol), hydrochloric acid (37 wt. % in water, 300 g, 250 mL, 3 mol) and water (400 mL). The reaction mixture was stirred at 5-10 °C, and sodium hypochlorite (14 wt % aqueous 35 solution, 522 g, 0.99 mol) was added over 2 h. The reaction mixture was maintained at 10-12 °C for 1 h until a Kl-starch paper test using sodium sulfite showed no remaining hypochlorite. The resulting mixture was cooled and filtered. The collected solid was washed WO 2006/121648 561399 PCT/US2006/016340 24 with cold water (160 mL), and dried to constant weight in a vacuum-oven at 50 °C to give 169 g (88 % yield) of the title compound as a solid melting at 189-190 °C. *H NMR (DMSO-d6) 8 13.4 (br s, 1H), 1.95 (m, 1H), 1.0 (m, 4H). Step C2: Another preparation of 5-chloro-2-cyclopropyl-l,6-dihydro-6-oxo-5 4-pyrimidinecarboxylic acid A 500 mL multi-neck flask with overhead stirrer, thermocouple and addition funnel was charged with 2-cyclopropyl-l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (36 g, 0.20 mol), water (70 mL) and 50 wt. % aqueous NaOH (14.4 g, 0.18 mol). The mixture was stirred at 10 °C, and 10.3 % aqueous NaOCl (160 g, 0.22 mol) was added over 1.5 h with 10 cooling to maintain the reaction mixture at 10 °C. The mixture was cooled to 5 °C, and sodium sulfite was added until Kl-starch paper gave negative test results. Hydrochloric acid (37 wt. % in water, 44.3 g, 0.443 mol) was added at 5 °C over about 30 minutes to lower the pH to 0.8. The mixture was filtered, and the collected solid was washed with cold 1 N HC1 (20 mL), and dried to constant weight in a vacuum-oven at 50 °C to give 40.9 g (95 % yield) 15 of the title compound as a solid melting at 189-190 °C. Step Dl: Preparation of 5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid Phosphorus oxychloride (363 g, 221 mL, 2.37 mol) and 5-chloro-2-cyclopropyl-l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (169 g, 0.79 mol) were added to a 1-L flask and heated at 90 °C for 5 h. The reaction mixture was cooled to 30 °C and added over 20 60 minutes into a 2-L jacketed reactor containing a well-stirred mixture of ?-butanol (280 mL) and water (750 mL) while maintaining the temperature at 5-10 °C. After the addition of the reaction mixture was about 70 % complete, the aqueous /-butanol mixture was seeded to initiate crystallization, and the addition of the reaction mixture was continued. At the end of the addition, water (750 mL) was added gradually at 10-15 °C, and the mixture 25 was stirred for an additional 1 h. The resulting mixture was cooled to 5 °C, filtered, and the collected solid was washed with water (3 x 50 mL). The resulting wet cake was dried in a vacuum-oven at 60 °C to give 156 g (85 % yield) of the title compound as a solid melting at 126-127 °C. NMR (DMSO-J6) 8 2.23 (m, 1H), 1.2 (m, 2H), 1.0 (m, 2H). 30 Step D2: Another preparation of 5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid A 500 mL multi-neck flask with overhead stirrer, thermocouple and condenser was charged with 5-chloro-2-cyclopropyl-l,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (35.0 g, 0.163 mol), ethyl acetate (105 mL) and JV,iV-dimethylformamide (1.19 g, 0.016 mol) 35 at room temperature. Thionyl chloride (48.5 g, 0.408 mol) was added at room temperature over 50 minutes, and the reaction mixture was heated at 68 °C for 7 h. The reaction mixture WO 2006/121648 561399 PCT/US2006/016340 25 was cooled to 25 °C and added over 30 minutes into a 500-mL multi-neck flask containing water (100 mL) while maintaining the temperature at 10-20 °C. The resulting mixture was stirred for additional 30 minutes, and the organic layer was separated from the aqueous layer. The aqueous layer was extracted with additional ethyl acetate (20 mL), and the combined 5 organic layers were washed with water. The organic layer containing 35.0 g (93% yield) of the title product was directly carried over to the next step. Step E: Preparation of 6-amino-5~chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid A 3-L flask was charged with 5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid (280 g, 1.2 mol), ammonia (28 wt % in water, 350 g, 5.76 mol) and water (1.26 L). The 10 reaction mixture was heated at 80 °C for 5 h, and excess water (about 600 mL) was removed by distillation at 50 °C/9 kPa. After cooling to 20 °C, the reaction mixture was acidified to pH 2 with aqueous hydrochloric acid (132 g, 110 mL, 1.32 mol), cooled to 5 °C, and filtered. The filtered wet cake was washed with water (2 x 200 mL) and dried in a vacuum-oven at 55 °C to give about 270 g of the title compound as a monohydrate, which contained 8.3 15 wt % of water measured by Karl Fischer titration, and decomposed at 152 °C (after crystallization from hot ethanol). !H NMR (DMSO-4,) 5 7.4 (br s, 3H), 1.9 (m, 1H), 0.9 (m, 4H). 13C NMR (DMSO-<%) 5 172.3,169.5, 163.9, 158.5,108.8, 21.1, 13.8. Step F1: Preparation of methyl 6-amino- 5-chloro-2-cyclopropyl-4-pyrimidine- 20 carboxylate A 1-L flask equipped with a nitrogen bubbler connected to a trap and caustic-containing scrubber, an addition funnel, reflux condenser and thermocouple, was charged with 6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid monohydrate (144 g, 0.62 mol) and methanol (500 mL). Thionyl chloride (185 g, 115 mL, 1.58 mol) was added 25 over about 30 minutes with cooling, and then the reaction mixture was heated at 60 °C for 12 h. The resulting mixture was concentrated at 40-45 °C/6 kPa to remove excess methanol (about 300 mL), and the reaction mixture was diluted with water (580 mL). Phenolphthalein (5 mg) was added, and 50 % aqueous NaOH (80 g, 1.0 mol) was added dropwise with cooling at 10-25 °C to bring the pH to about 9 as indicated by appearance of pink color. 30 - Then just enough 1 N aqueous hydrochloric acid was added to extinguish the pink color. The resulting slurry was cooled to 5 °C and filtered. The filtered wet cake was washed with water and dried to constant weight at 50 °C/6 kPa to give 123 g (80 % yield) of the title compound with 98 % purity by HPLC analysis as a solid melting at 147-148 °C. !H NMR (DMSO-d6) 5 5.4 (br s, 2H), 3.97 (s, 3H), 2.1 (m, 1H), 1.04 (m, 4H). 35 The remaining filtrate was acidified with hydrochloric acid (37 wt. % in water) to bring the pH to about 2, and then concentrated in vacuo. The resulting slurry was filtered, WO 2006/121648 561399 PCT/US2006/016340 26 washed with water, and dried to give 14 g of unreacted 6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid (10 % recovered yield). Step F2: Another preparation of methyl 6-amino-5-chloro-2-cyclopropyl-4-pyrimidine-carboxylate 5 A 500 mL multi-neck flask equipped with nitrogen bubbler, addition funnel, reflux condenser, and thermocouple was charged with 6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid monohydrate (47.8 g, 0.206 mol), methanol (32 g) and dimethyl carbonate (94.5 g, 1.05 mol). Concentrated sulfuric acid (50.0 g, 0.500 mol) was added over about 30 minutes with cooling to maintain the temperature below 60 °C, and then the 10 reaction mixture was heated at 70 °C for 10 h. The resulting mixture was cooled to 15 °C and diluted with 250 ruL of water. The pH of the reaction mass was raised to 5-8 by adding about 42.7 g (0.534 mol) of 50 wt % aqueous NaOH over 30 minutes with cooling to maintain the temperature in the range of 10-15 °C. The resulting slurry was cooled to 5 °C and filtered. The filtered wet cake was washed with water and dried to constant weight at 15 50 °C to give 43.3 g (93.5 % yield) of the title compound with 98 % purity as a solid melting at 147-148 °C. Step F3: Another preparation of methyl 6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylate A 200-mL reactor equipped with a 10-mL jacketed addition funnel below a 20 cold-finger condenser at -10 °C, a nitrogen inlet and overhead stirring was charged with tributylamine (20.4 g, 0.11 mol) and DMSO (45 mL). The mixture was stirred at 25 °C, and 6-amino-5-chloro-2-cyclopropyI-4-pyrimidinecarboxylic acid monohydrate (23.1 g, 0.1 mol) was added in portions. The reaction mixture was stirred at 30 °C while bromomethane (13.3 g, 8 mL, 0.14 mol) was condensed into the jacketed addition funnel and then added to 25 the reaction mixture over 30 minutes. The mixture was stirred for an additional 3 h and then added over about 30 minutes to a reactor charged with water (200 mL) at 25 °C. The resulting slurry was cooled to 5 °C and filtered. The filtered cake was washed with water (2 x 30 mL) and dried at 60 °C in a vacuum-oven for 16 h to give 18.4 g (81 % yield) of the title compound as an off-white solid melting at 147-148 °C. 30 By the present method, the following compounds of Tables 1-4 can be prepared. The following abbreviations are used in the Table which follow: t means tertiary, i means iso, Me means methyl, Et means ethyl, Pr means propyl, z-Pr means isopropyl, e-Pr means cyclopropyl, Bu means butyl, z-Bu means isobutyl, and S(0)2Me means methylsulfonyl. WO 2006/121648 561399 PCT/US2006/016340 27 TABLE 1 R HN o N C02H r1 z-Pr c-Pr 2-Me-c-Pr /-Bu Ph 4-Cl-Ph 3-Cl-Ph 4-Br-Ph 4-F-Ph 2-F-Ph r! 4-I-Ph 3-Me-Ph 4-Et-Ph 4-CF3-Ph 4-Me-Ph 3,4-di-Cl-Ph 2,4-di-Cl-Ph 2-F-4-Cl-Ph 3,4-di-Me-Ph 3-F-4-Me-Ph r! 4-MeO-Ph 4-MeS-Ph 4-CF30-Ph 3-Br-5-MeO-Ph 4-MeS(0)2-Ph 4-MeS(0)-Ph 1,3-benzodioxol-5 -yl 2-naphthalenyl TABLE 2 Rl 7-Pr c-Pr 2-Me-c-Pr z'-Bu Ph 4-Cl-Ph 3-Cl-Ph 4-Br-Pli 4-F-Ph 2-F-Ph R1 N C02H El 4-I-Ph 3-Me-Ph 4-Et-Ph 4-CF3-P1i 4-Me-Ph 3,4-di-Cl-Ph 2,4-di-Cl-Ph 2-F-4-Cl-Ph 3,4-di-Me-Ph 3-F-4-Me~Ph •El 4-MeO-Ph 4-MeS-Ph 4-CF30-Ph 3-Br-5-MeO-Ph 4-MeS(0)2-Ph 4-MeS(0)-Ph 1,3 -benzodioxol-5-yl 2-naphthalenyl WO 2006/121648 561399 PCT/US2006/016340 28 TABLE 3 XX R1 N "C09H r! z-Pr c-Pr 2-Me-c-Pr z'-Bu Ph 4-Cl-Ph 3-Cl-Ph 4-Br-Ph 4-F-Ph 2-F-Ph r! 4-I-Ph 3-Me-Ph 4-Et-Ph 4-cf3-PI1 4-Me-Ph 3,4-di-Cl-Ph 2,4-di-Cl-Ph 2-F-4-Cl-Ph 3,4-di-Me-Ph 3-F-4-Me-Ph El . 4-MeO-Ph 4-MeS-Ph 4-CF30-Ph 3-Br-5-MeO-Ph 4-MeS(0)2-Ph 4-MeS(0)-Ph 1,3-benzodioxol-5-yl 2-naphthalenyl TABLE 4 NH2 CI N" | R1^>N/^co2R4 r1 E1 c-Pr CH2CH3 c-Pr CH3 c-Pr H c-Pr /-Pr c-Pr CH2CH2CH3 c-Pr CH2CH2CH2CH3 c-Pr z'-Bu c-Pr CH2Ph c-Pr CH2CH20(«-Bu) c-Pr CH2CH2OCH2CH2OCH3 c-Pr CH2CH2CH2OH El E4 c-Pr (CH2)7ch3 c-Pr CH(CH3)(CH2)5ch3 c-Pr CH2CH(C2H5)(CH2)3CH3 2-Me-c-Pr CH3 /-Pr CH2CH3 /-Pr CH3 z'-Bu CH2CH3 Ph CH2CH3 Ph CH3 4-Cl-Ph CH2CH3 4-Cl-Ph CH3 </div>

Claims

<div class="application article clearfix printTableText" id="claims"> WO 2006/121648 561399 PCT/US2006/016340 El g4 El rl 4-Cl-Ph h 4-CF3-Ph ch2ch3 4-Cl-Ph z-Pr 4-CF3-Ph ch3 4-Cl-Ph ch2ch2ch3 3-CF3-Ph ch2ch3 4-Cl-Ph CH2Ph 4-Me-Ph ch2ch3 3-Cl-Ph ch2ch3 3,4-di-Cl-Ph ch2ch3 4-Br-Ph ch2ch3 2,4-di-Cl-Ph ch2ch3 4-Br-Ph ch3 2-F-4-Cl-Ph ch2ch3 4-Br-Ph H 3,4-di-Me-Ph ch2ch3 4-F-Ph ch2ch3 3-F-4-Me-Ph ch3 4-F-Ph ch3 3-F-4-Me-Ph H 4-F-Ph H 4-MeO-Ph ch2ch3 2-F-Ph ch2ch3 4-MeS-Ph ch3 4-I-Ph ch2ch3 4-CF30-Ph ch2ch3 4-I-Ph ch3 3-Br-5-MeO-Ph ch2ch3 4-Me-Ph ch3 4-MeS(0)2-Ph ch3 4-Me-Ph H 4-MeS(0)-Ph ch3 3-Me-Ph ch3 1,3-benzodioxol-5-yl ch2ch3 4-Et-Ph ch2ch3 2-naphthalenyl ch2ch3 5613,99 30 The claims defining the invention are as follows:

1. A method for preparing a compound of Formula 1, hA > 1 ^7 r1 N 1 -co2H wherein R1 is optionally substituted cyclopropyl or an optionally substituted phenyl; comprising the steps of: (1) contacting a mixture comprising (a) a compound of Formula 2a r2o2c *co2r3 om 2a wherein m is alkali metal and R2 and R3 are independently C1-C4 alkyl, (b) a C1-C4 alkanol, and (c) a first portion of water, with a solution comprising a first base and a second portion of water, said base being in an amount sufficient to create a first resultant solution having a pH ranging from about 10 to about 14, said first resultant solution comprising a compound of Formula 2b, mo2c. xo2Rj om 2b wherein m and R3 are defined as above for Formula 2a; (2) contacting the first resultant solution comprising the compound of Formula 2b with a compound of Formula 3 or an acid salt thereof or with a solution comprising a compound of Formula 3 or an acid salt thereof, nh X r1nh2 wherein R1 is defined as above for Formula 1, and a second base in an amount sufficient to create a second resultant solution having a pH ranging from about 9 to about 12, said second resultant solution comprising a salt of the compound of Formula 1; and intellectual property office of n.z. -7 OCT 2009 RECEIVED 561399 31 (3) adding an acid to the second resultant solution comprising the salt of the compound of Formula 1 to form the compound of Formula 1.

2. The method of Claim 1 wherein R1 is optionally substituted cyclopropyl.

3. The method of Claim 2 wherein R5 is cyclopropyl.

4. The method of Claim 1 wherein the first base added in step (1) is an alkali metal hydroxide.

5. The method of Claim 4 wherein the alkali metal hydroxide is sodium hydroxide or potassium hydroxide.

6. The method of Claim 1 wherein the pH of the first resultant solution in step (1) is in a range of 11 to 13.

7. The method of Claim 1 wherein the molar ratio of the compound of Formula 3 or an acid salt thereof to the compound of Formula 2a is in a range of 0.7 to 0.9.

8. The method of Claim 1 wherein the second base added in step (2) is an alkali metal hydroxide.

9. The method of Claim 8 wherein the alkali metal hydroxide is sodium hydroxide or potassium hydroxide.

10. The method of Claim 1 wherein the pH of the second resultant solution in step (2) is in a range of 10.5 to 11.5.

11. The method of Claim 1 wherein the acid added in step (3) is a mineral acid.

12. The method of Claim 11 wherein the acid is sulfuric acid or hydrochloric acid.

13. A method for preparing a compound of Formula 4 wherein R1 is H or an optionally substituted carbon moiety, comprising the method of Claim 1 and a further step comprising contacting the compound of Formula 1 with a chlorinating agent.

14, A method for preparing a compound of Formula 6 O R1 m UC2H 4 intellectual property office of n.z. -7 OCT 2009 received 561399 32 CI n' R n 6 CI Xo2b wherein R1 is H or an optionally substituted carbon moiety, comprising the method of Claim 13 and a further step comprising contacting the compound of Formula 4 with a chloride displacement agent.

15. A method for preparing a compound of Formula 7 NH, ■ n CI xo2h wherein R1 is H or an optionally substituted carbon moiety, comprising the method of Claim 14 and a further step comprising contacting the compound of Formula 6 with ammonia.

16, A method of preparing a compound of Formula 8 NH2 IT R1 N''X;O2R4 8 wherein R1 is H or an optionally substituted carbon moiety; and R4 is an optionally substituted carbon moiety; comprising the method of Claim 15 and an additional step of contacting the compound of Formula 7 with an R4 transfer agent. intellectual property office of n.z. - 7 OCT 2009 RECEIVED 561399 33

17. A method for preparing a compound of Fonmula 4 O HN-VC1 R1 N C02H wherein R1 is H or an optionally substituted carbon moiety, using a compound of Formula 1, hA A JL R1 n x02h 1 characterized by: preparing the compound of Formula 1 by the method of Claim 1.

18. A method for preparing a compound of Formula 6 CI ,c1 XX rl n co2h 6 wherein R1 is H or an optionally substituted carbon moiety, using a compound of Formula 1 O hA A k r n c02h characterized by: preparing the compound of Formula 1 by the method of Claim 1. intellectual property office of n.z. - 7 OCT 2009 RECEIVED 561399 34

19. A method for preparing a compound of Formula 7 NH2 „Cl N ,1^-, R1 N C02H 7 wherein R1 is H or an optionally substituted carbon moiety, using a compound of Formula 1 O HN' niN |i R1^^N "vco2H characterized by; preparing the compound of Formula 1 by the method of Claim 1.

20. A method for preparing a compound of Formula 8 NH2 ^C1 N R1^ ^N CO?R4 8 wherein R1 is H or an optionally substituted carbon moiety; and R4 is an optionally substituted carbon moiety; using a compound of Formula 1 O rnfS aJL HN A R1 N^ >C02H 1 characterized by: preparing the compound of Formula 1 by the method of Claim 1. intellectual property office of n.z. -? OCT 2009 RECEIVED 561399 35

21. The method of any one of Claims 16 and 20 wherein R4 is C1-Cj4 alkyl, C2-C14 alkoxyalkyl, C2-Ci4 hydroxyalkyl or benzyl.

22. The method of Claim 21 wherein R4 is Cj-Cg alkyl or C2-Cg alkoxyalkyl.

23. The method of Claim 22 wherein R4 is Cj-C4 alkyl.

24. The method of any one of Claims 1 to 23 wherein R1 is cyclopropyl.

25. The method of any one of Claims 1 to 24 substantially as hereinbefore described with reference to the accompanying Examples. intellectual property OFFICE OF N.2. - 7 OCT 2009 RECEIVED </div>